Phenylephrine Hydrochloride Injectable Solution, 40mg, 250*ml Bag, Wells Pharma Of Houston
Wells Pharma of Houston is recalling Phenylephrine Hydrochloride Injectable Solution 40mg in 250mL bags nationwide because the product was manufactured with deviations from required quality standards. This injectable medication is used to treat low blood pressure and was distributed across all U.S. states. Healthcare facilities and pharmacies that received this product should check their inventory against the recall details.
- Recalling firm
- Wells Pharma of Houston LLC
- Product
- Phenylephrine Hydrochloride Injectable Solution, 40mg, 250*mL Bag, wells pharma of Houston, NDC 73702-122-03
- Reason
- cGMP deviations.
- Classification
- Class II
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-04-01
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- U.S. Nationwide.
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/cbe3afb5-551d-40de-8ab2-4ca64797cd82